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IFT52基因中的纯合无义变异与一种人类骨骼纤毛病相关。

A homozygous nonsense variant in IFT52 is associated with a human skeletal ciliopathy.

作者信息

Girisha K M, Shukla A, Trujillano D, Bhavani G S, Hebbar M, Kadavigere R, Rolfs A

机构信息

Department of Medical Genetics, Kasturba Medical College, Manipal University, Manipal, India.

Department of Bioinformatics, Centogene AG, Rostock, Germany.

出版信息

Clin Genet. 2016 Dec;90(6):536-539. doi: 10.1111/cge.12762. Epub 2016 Mar 15.

Abstract

Intraflagellar transport (IFT) is vital for the functioning of primary cilia. Defects in several components of IFT complexes cause a spectrum of ciliopathies with variable involvement of skeleton, brain, eyes, ectoderm and kidneys. We examined a child from a consanguineous family who had short stature, narrow thorax, short hands and feet, postaxial polydactyly of hands, pigmentary retinopathy, small teeth and skeletal dysplasia. The clinical phenotype of the child shows significant overlap with cranioectodermal dysplasia type I (Sensenbrenner syndrome). Whole-exome sequencing revealed a homozygous nonsense variant p.R142* in IFT52 encoding an IFT-B core complex protein as the probable cause of her condition. This is the first report of a human disease associated with IFT52.

摘要

鞭毛内运输(IFT)对于初级纤毛的功能至关重要。IFT复合体的几个组分缺陷会导致一系列纤毛病,骨骼、大脑、眼睛、外胚层和肾脏会有不同程度的受累。我们检查了一名来自近亲家庭的儿童,其表现为身材矮小、胸廓狭窄、手足短小、手部轴后多指畸形、色素性视网膜病变、牙齿小和骨骼发育异常。该儿童的临床表型与I型颅外胚层发育不良(森森布伦纳综合征)有显著重叠。全外显子组测序显示,编码IFT - B核心复合体蛋白的IFT52基因存在纯合无义变异p.R142*,这可能是导致其病症的原因。这是与IFT52相关的人类疾病的首例报告。

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